{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Eberbach",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90743",
      "recalling_firm": "GELITA MEDICAL GMBH",
      "address_1": "Uferstr. 7",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of Alabama.",
      "recall_number": "Z-1768-2022",
      "product_description": "ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM",
      "product_quantity": "3596 boxes of 50 devices",
      "reason_for_recall": "In routine bioburden testing, higher than acceptable levels of Endotoxins were observed.",
      "recall_initiation_date": "20220727",
      "center_classification_date": "20220919",
      "report_date": "20220928",
      "code_info": "UDI/DI 00860003109915, Batch Numbers:  T02371/1, expiration date 10.02.2026; T02371/2, expiration date 10.02.2026; T02395/1, expiration date 07.05.2026; T02394/2, expiration date 07.05.2026"
    }
  ]
}